Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10046
rs10046
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.100 0.818 11 2008 2018
dbSNP: rs4646
rs4646
0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.090 1.000 9 2008 2015
dbSNP: rs700519
rs700519
0.752 0.280 15 51215771 missense variant G/A snv 7.6E-02 8.0E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.070 0.714 7 2003 2016
dbSNP: rs2236722
rs2236722
0.851 0.120 15 51242798 missense variant A/G snv 3.4E-03 9.1E-04
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.040 1.000 4 2002 2010
dbSNP: rs4775936
rs4775936
0.790 0.200 15 51243825 intron variant C/T snv 0.36
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.030 0.667 3 2008 2019
dbSNP: rs700518
rs700518
0.732 0.320 15 51236915 synonymous variant T/C snv 0.43 0.40
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.030 1.000 3 2014 2015
dbSNP: rs1008805
rs1008805
0.851 0.160 15 51257402 intron variant G/A snv 0.64
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 2008 2017
dbSNP: rs1004982
rs1004982
0.925 0.080 15 51321614 non coding transcript exon variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11856927
rs11856927
0.925 0.080 15 51256508 intron variant G/T snv 0.58
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1413421847
rs1413421847
0.882 0.160 15 51242801 missense variant C/T snv 2.8E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2009 2009
dbSNP: rs28566535
rs28566535
0.851 0.120 15 51308944 intron variant A/C;G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs3751591
rs3751591
0.925 0.080 15 51314513 intron variant A/G snv 0.13
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7176005
rs7176005
0.925 0.080 15 51339082 upstream gene variant C/T snv 0.21
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs730154
rs730154
0.925 0.080 15 51299007 intron variant T/C snv 0.30
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs774053181
rs774053181
0.925 0.080 15 51242874 missense variant G/C snv 4.0E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs936306
rs936306
0.925 0.080 15 51287401 intron variant C/T snv 0.30
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008